Anti-fouling cationically crosslinkable varnish compositions and support substrates coated therewith

ABSTRACT

Silicone compositions particularly useful for the production of anti-fouling varnishes for application to support substrates, these providing an anti-fouling varnish for textiles covered with silicone elastomers which is economical, adhesive, non-slip and glossy; the subject varnishes comprise a crosslinkable silicone composition containing, per 100 parts by weight: 1, at least 80 parts by weight of: (1.1), 2., 0.1 to 10 parts of weight of: (1.2), 3., 0 to 10 parts by weight of at least one polydimethylisiloxane (PDMS) acrylate or epoxide, 4., 0 to 10 parts by weight of at least one silylated compound which includes at least one ultrafine filler, 7., 0 to 10 parts by weight of at least one thickener, and 8., 0 to 10 parts by weigh of at least one additional functional additive.

CROSS-REFERENCE TO PRIORITY/PCT APPLICATIONS

This application is a divisional of U.S. application Ser. No.11/166,380, filed Jun. 27, 2005, which claims priority under 35 U.S.C.§119 of FR 02/16713, filed Dec. 26, 2002, and is a continuation ofPCT/FR 2003/003618, filed Dec. 8, 2003 and designating the United States(published in the French language on Aug. 12, 2004 as WO 2004/067620 A1;the title and abstract were also published in English), each herebyexpressly incorporated by reference and each assigned to the assigneehereof.

CROSS-REFERENCE TO COMPANION APPLICATION

Our copending application Ser. No. 11/166,218, filed Jun. 27, 2005 andalso assigned to the assignee hereof.

BACKGROUND OF THE INVENTION

1. Technical Field of the Invention

The present invention relates to polymer coatings or varnishes able toconfer, in particular, anti-fouling properties to supports, especially:

flexible support substrates, in particular fibrous, woven or nonwovensupports, that may or may not be coated with at least one mechanicalreinforcement or protective layer, based on a coating polymer of thesilicone elastomer type, for example;

bulk supports made of silicone and/or coated with one or more layers ofsilicone, for example metal, plastic or ceramic parts (e.g., electricalinsulators);

or else polymeric or elastomeric supports, in particular plastic films,for instance: thermal transfer ribbons for use in particular as an inksupport in heat transfer printers; or protective packaging films.

These supports may optionally at least partly be made of silicone.

The present invention also relates to methods for applying theanti-fouling varnish, to which it relates, onto various supports.

Too, this invention also relates to supports coated with suchanti-fouling varnishes, and in particular flexible supports such astextile cloths coated with a layer of silicone elastomer to which theanti-fouling varnish is applied, such cloths being useful for producing:

1. architectural textiles (elements of textile architecture);

2. or else flexible supports other than architectural textiles.

As regards the field of application 1, it should be appreciated that,throughout the present disclosure and for the purposes of the presentinvention, the term “architectural textile” means a woven or nonwovenfabric, and more generally any fibrous support useful, after coating,for making up:

shelters, movable structures, textile buildings, partitions, flexibledoors, tarpaulins, tents, stands or marquees;

furniture, claddings, billboards, windshields or filter panels;

solar protection panels, ceilings and blinds.

As regards the field of application 2, it will be appreciated that theseflexible supports other than architectural textiles may, for example, bethose intended for the production in particular of:

airbags used for protecting the occupants of a vehicle,

glass braids (woven glass sheets for thermal and dielectric protectionfor electrical wires),

conveyor belts, fire-barrier or thermal insulation fabrics,

clothing,

compensators (flexible sealing sleeves for pipe work), etc.

Because of the intrinsic properties of silicones, the silicone elastomercoatings on textile supports already provide the composites thus formedwith many advantages, namely, inter alia:

flexibility,

mechanical strength,

heat resistance,

and longevity.

However, in the field of textile architecture, which constitutes animportant application for the abovementioned composites, otherrequirements have been formulated, which are in particular thefollowing:

resistance to fouling,

ability to bond so as to allow ready assembly of the composites two bytwo (for example, with an adhesive force F≧70 N/5 cm, and preferablyF≧120 N/5 cm),

low slip coefficient so as to promote handling of the composite, forexample equivalent to a Kd≦0.8,

good characteristics of appearance, in particular with regard to colorand gloss,

good cohesion of the composite.

These properties can be provided by a varnish. The general problemforming the basis of the invention is therefore the development of asilicone varnish able to fully accomplish this role, in particular withregard to anti-fouling qualities.

However, before satisfying the requirements relating to the finalapplications intended for the composite, it is important for thisvarnish to satisfy, moreover, upstream specifications, namely, inparticular:

to be able to be readily spread over a silicone layer,

to adhere completely to this silicone layer,

and more generally, to be easy and economical to use in industrialterms.

2. Description of Background and/or Related and/or Prior Art

WO-A-00/59992 describes silicone compositions that are especially usefulfor producing varnishes which can be applied to supports whose frictioncoefficient it is desired to decrease.

One of these compositions comprises:

at least one polyorganosiloxane (POS) A that is crosslinkable by meansof crosslinking functional groups (CFGs) via the cationic and/or radicalpathway:

an initiator C selected from onium borates:

C=

and at least one silylated compound D substituted with secondaryfunctional groups (SFGs), preferably of alkoxy type, carried by siliconatoms and selected from those comprising at least one alkoxy and/orepoxy and/or carboxyl unit, and optionally CFGs of (meth)acrylate and/orvinyl ether and/or epoxide and/or oxetane, preferably epoxide, type;they may, for example, be the following compounds:

-   -   silane of type:

-   -   POS of type:

and, optionally, a filler (e.g., silica), for example: pyrogenic silicastreated with hexamethyldisilazane or with octamethylcyclotetrasiloxane(specific surface area up to approximately 300 m²/g), fumed silicas,ground synthetic or natural fibers (polymers), calcium carbonates, talc,clays, titanium dioxides, etc.

Such compositions are used as anti-fouling varnishes for RTV siliconecoatings of fabrics for airbags, for thermal transfer ribbons or forpackaging films.

Such varnishes can be improved in terms of anti-fouling properties, ofbonding ability, or even of reduction in slip coefficient. In addition,they require the use of specific silicones that are crosslinkable viathe cationic pathway with UV activation, which leaves a margin forimprovement in economic terms and in terms of simplification of themeans implemented.

It therefore appears that the prior art is essentially devoid ofanti-fouling varnishes compatible with silicone elastomer coatings forsupports, in particular textile supports, and even less so inanti-fouling varnishes that satisfy the above specifications.

SUMMARY OF THE INVENTION

Novel anti-fouling varnish compositions for various silicone-comprisingsupports have now been developed, in particular for flexible (textile)supports coated with silicone elastomers or bulk supports made ofsilicone elastomer, the essential qualities of such varnish compositionsbeing those of having good resistance to fouling and of allowingassembly by bonding of the parts to which it is applied.

Another aspect of the present invention is the provision of anti-foulingand “bondable” varnishes that impart the non-slip surface desired, whichis completely anchored on the support, and in particular on the layer ofcoated elastomer, and which has a glossy appearance, while at the sametime remaining economical.

Another aspect of the present invention is to provide anti-foulingvarnishes that can be readily applied to various types of supports.

Another aspect of the invention is to provide crosslinkable anti-foulingvarnishes that are easy to use and economical.

Another aspect of the present invention is to provide varnishcompositions essentially based on nonsilylated species and yetcompatible with silicone elastomers and useful, in particular, forproducing anti-fouling varnishes, these compositions having a reasonablecost and being simple to prepare.

Another aspect of the invention is to provide a method for the simpleand economical varnishing of various silicone-comprising or siliconesupports made up, for example, of woven or nonwoven fibrous substratescoated with a layer of crosslinked silicone elastomer, or of bulksupports at least in part being made of silicone, using an anti-foulingvarnish based on silylated species compatible with silicone elastomers.

Another aspect of the invention is to provide a composite comprising asupport coated with at least one layer of elastomer and covered with asilicone varnish as defined above, for example a cloth (architecturaltextile) coated with crosslinked silicone elastomer, with highresistance to fouling.

Thus, to satisfy the above objectives, the present invention featuresfirstly, varnishes that are polymerizable/crosslinkable via the cationicroute, in particular having anti-fouling properties, and comprising, per100 parts by weight:

1. at least 80 parts by weight of at least one basic compoundcomprising, per molecule, at least two polymerization/crosslinkinggroups, at least one of these groups being selected from among thefollowing groups: alkenyl ether, epoxy, oxetane; these two groupspreferably being selected from the group consisting of the followingcombinations of groups: epoxy-epoxy, oxetane-hydroxyl,oxetane-alkoxysilyl, carboxyl-oxetane, oxetane-oxetane, alkenylether-hydroxyl, epoxy-alkoxy, and epoxy-alkoxysilyl;

2. from 0.1 to 10 parts by weight of at least one cationic initiatorselected from among those for which the cationic moiety is selected fromamong onium salts of formula (I):[(R¹)_(n)-A-(R²)_(m)]⁺  (I)in which A is an element of groups 15 to 17 of the Periodic Table, forinstance: I, S, Se, P or N; R¹ is a C₆-C₂₀ carbocyclic or heterocyclicaryl radical, said heterocyclic radical optionally containing asheteroelements, nitrogen or sulfur; R² is R¹ or a C₁-C₃₀ linear orbranched alkyl or alkenyl radical, said radicals R¹ and R² optionallybeing substituted with a C₁-C₂₅ alkoxy, C₁-C₂₅ alkyl, nitro, chloro,bromo, cyano, carboxyl, ester or mercapto group; n is an integer rangingfrom 1 to v+1, v being the valency of the element A, and m is an integerranging from 0 to v−1 with n+m=v+1; and for which the anionic moiety ofthe initiator is a borate of formula (II):[BX_(a)R_(b)]⁻  (II)in which a and b are integers ranging, for a, from 0 to 3 and, for b,from 1 to 4, with a+b=4; the symbols X represent:

a halogen (chlorine, fluorine) atom with a=0 to 3,

an OH function with a=0 to 2, and the symbols R, which are identical ordifferent, are each:

a phenyl radical substituted with at least one electron-withdrawinggroup, for instance OCF₃, CF₃, NO₂ or CN, and/or with at least 2 halogen(most particularly fluorine) atoms, this being the case when thecationic entity is an onium of an element of groups 15 to 17,

a phenyl radical substituted with at least one element or one group thatis electron-withdrawing, in particular halogen (most particularlyfluorine) atoms, CF₃, OCF₃, NO₂ or CN, this being the case when thecationic entity is an organometallic complex of an element of groups 4to 10,

an aryl radical containing at least two aromatic rings, for instancebiphenyl, naphthyl, optionally substituted with at least one element orone group that is electron-withdrawing, in particular a halogen atom,including fluorine in particular, OCF₃, CF₃, NO₂ or CN, whatever thecationic entity, this initiator preferably being selected from the groupconsisting of:[(Φ)₂I]⁺, [B(C₆F₅)₄]⁻[(C₈H₁₇)—O-Φ-I-Φ)]⁺, [B(C₆F₅)₄]⁻[(C₁₂H₂₅-Φ-I-Φ]⁺, [B(C₆F₅)₄]⁻[(C₈H₁₇—O-Φ)₂I]⁺, [B(C₆F₅)₄]⁻[(C₈H₁₇)—O-Φ-I-Φ)]⁺, [B(C₆F₅)₄]⁻[(Φ)₃S]⁺, [B(C₆F₅)₄]⁻[(Φ)₂S-Φ-O—C₈H₁₇]⁺, [B(C₆H₄CF₃)₄]⁻[(C₁₂H₂₅-Φ)²I]⁺, [B(C₆F₅)₄]⁻[(CH₃)₂—CH-Φ-I-Φ-CH₃]⁺, [B(C₆F₅)₄]⁻(η⁵-cyclopentadienyl)(η⁶-toluene)Fe⁺, [B(C₆F₅)₄]⁻(η⁵-cyclopentadienyl)(η⁶-methyl-1-naphthalene)Fe⁺, [B(C₆F₅)₄]⁻(η⁵-cyclopentadienyl)(η⁶-cumene)Fe⁺, [B(C₆F₅)₄]⁻

nontoxic onium salt with a cationic structure of formula (III):[(CH(CH₃)₂-Φ-)-I—(—R³)]⁺  (III)in which the symbol R³ represents the radical -Φ-R⁴, R⁴ being a linearor branched alkyl radical having from 1 to 20 carbon atoms, preferably 1to 15 carbon atoms,and having an anionic structure selected from the group consisting of:

Cl⁻, Br⁻, BF₄ ⁻, PF₆ ⁻, CF₃SO₃ ⁻, N(SO₂CF₃)₂ ⁻, C(SO₂SF₃)₂ ⁻, B(C₆F₅)₄⁻, B(PhOCF₃)₄ ⁻, SbF₆ ⁻, and/or AsF₆ ⁻;

3. from 0 to 10 parts by weight of at least one polyorganosiloxane (POS)other than the basic compound 1. and substituted, per molecule, by atleast one alkenylated group, preferably (meth)acrylic or a salt thereof,and/or at least one epoxy group;

4. from 0 to 10 parts by weight of at least one silylated compoundsubstituted, per molecule, by at least one epoxy group;

5. from 0 to 10 parts by weight of at least one silylated compoundsubstituted, per molecule, by at least one alkenylated group, preferably(meth)acrylic or a salt thereof, and at least one epoxy, alkenyl etheror oxetane group, with the following provisos:

-   -   a) the additive 3. and the additive 4. are necessarily present        in the absence of additive 5.;    -   b) and the alkenylated-epoxidized additive 5. is necessarily        present in the absence of additives 3. and 4.;

6. from 0 to 10 parts by weight of at least one ultrafine filler;

7. from 0 to 10 parts by weight of at least one thickener;

8. from 0 to 10 parts by weight of at least one other functionaladditive.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 illustrates a fouling scale according to a comparison withinfra-type micrographs.

DETAILED DESCRIPTION OF BEST MODE AND SPECIFIC/PREFERRED EMBODIMENTS OFTHE INVENTION

The varnishes according to the invention are advantageous in that theymake it possible to very greatly increase the resistance to fouling andthe bonding ability, while at the same time having a low slipcoefficient and a glossy appearance.

The mechanical qualities and the operating properties of the supportsvarnished by means of the varnishes according to the invention are notaffected.

In addition, the subject varnishes are stable.

Preferred combinations of components according to the invention are:1/2/3/4 and 1/2/5, optionally combined with 6 and/or 7 and/or 8. This isbecause, it could not have been predicted that this combination ofjudiciously selected components might provide all the abovementionedadvantageous results.

The term “alkenyl” means a substituted or unsubstituted, linear orbranched, unsaturated hydrocarbon-based chain having at least one olefindouble bond, and more preferably a single double bond. Preferably, the“alkenyl” group has from 2 to 8 carbon atoms, better still from 2 to 6.This hydrocarbon-based chain optionally comprises at least oneheteroatom such as O, N or S.

Preferred examples of “alkenyl” groups are vinyl, allyl and homoallylgroups, vinyl being particularly preferred.

In accordance with the invention, preference may be given to the basiccompounds 1. selected from:

1.1 those for which the polymerization/crosslinking groups are oxetanes,and preferably from the epoxy monomers having the formula below:

1.2 or those containing at least one crosslinkable and/or polymerizablesilicone oligomer and/or polymer that is liquid at ambient temperatureor thermofusible at a temperature below 100° C., the silicone oligomerand/or polymer comprising:

-   -   at least one structural unit of formula (1.2):        Z(R⁰)_(a)SiO_(3-a/2)  (1.2)        in which:

a=0, 1 or 2,

the radicals R⁰, which may be identical or different, are each an alkyl,cycloalkyl, aryl, vinyl, hydroxyl or alkoxy radical, or hydrogen atom,preferably a C₁-C₆ lower alkyl radical,

Z is an organic substituent comprising at least one epoxy, and/oralkenyl ether and/or oxetane and/or dioxolane and/or carbonate reactivefunction,

and at least two silicon atoms.

The reactive functions Z of the silicone polymer or oligomer 1.2 may bevery varied. However, particularly advantageous varnishes are obtainedwhen the silicone oligomer or polymer (1.2) comprises at least one (SF)unit in which Z represents an organic substituent Z1 comprising at leastone epoxy and/or dioxolane reactive function, and preferably at leastone epoxy reactive function.

According to two advantageous alternative embodiments of the presentinvention, the silicone oligomer or polymer 1.2 with at least one epoxyand/or dioxolane reactive function Z1, and preferably at least one epoxyreactive function Z1, can:

(i) either comprise only this or these type(s) of reactive function(s)Z1,

(ii) or comprise other reactive functions Z, such as alkenyl ether,oxetane and/or carbonate reactive functions Z2.

In the case of the first alternative (i), the varnish can also compriseother silicone oligomers and/or polymers that are different from theoligomer/polymer 1.2, comprising other reactive functions Z2, such asalkenyl ether, oxetane and/or carbonate functions, and, optionally,reactive functions Z1.

By way of examples of reactive functions Z, these may in particular beselected from among the following radicals:

with R″ representing a C₁-C₆ linear or branched alkyl radical.

According to a second advantageous embodiment of the present invention,the silicone polymer or oligomer 1.2 comprises at least one siliconehaving the average formula below:

In these formulae, R₀ or (R)⁰=alkyl (preferably C₁-C₁₀) or aryl(preferably phenyl).

According to a preferred embodiment of the invention, the cationicinitiator 2. is selected from the group comprising:[((CH₃)₂—CH-Φ-)-I-Φ-CH₃]⁺Cl⁻[((CH₃)₂—CH-Φ-)-I-Φ-CH₃]⁺B(C₆F₅)₄ ⁻[((CH₃)₂—CH-Φ-)-I-Φ-CH₃]⁺PF₆ ⁻[(CH₃)₂—CH—CH₂-Φ-)-I-Φ-CH₃]⁺PF₆ ⁻[(CH₃)₂—CH—CH₂-Φ-)-I-Φ-CH₃]⁺B(C₆F₅)₄ ⁻[(CH(CH₃)₂-Φ-)-I-Φ-CH₃]⁺B(PhOCF₃)₄ ⁻

and mixtures thereof.

According to another preferred embodiment of the invention, the additive3. is:

3.1 at least one alkenylated polyorganosiloxane (POS) in which thealkenyl groups each comprise at least one (meth)acrylic or(meth)acrylate function, said alkenyl groups being more particularlyselected from the groups having the general formula below:

in which:

R⁴ and R⁵ are hydrogenated or hydrocarbon-based radicals that areidentical to or different from one another and preferably representhydrogen, a C₁-C₄ linear or branched alkyl radical or a phenyl radicaloptionally substituted with at least one C₁-C₃ alkyl radical,

R⁶ is methyl or a hydrogen atom, the additive 3.1 being even moreespecially selected from (poly)(meth)acrylate POSs;

3.2 and/or at least one epoxidized POS other than the basic compound 1.

The (poly)(meth)acrylate POSs are polyorganosiloxanes comprising, permolecule, one or more acrylate or methacrylate functionalities. Althoughthe terms “acrylate” and “methacrylate” denote more specifically acrylicacid esters and methacrylic acid esters, they are also, according to theinvention, directed toward the acid forms as such.

By way of examples of (poly)(meth)acrylate POSs, a certain number ofbibliographical references describing them are indicated hereinafter.

FR-A-2,377,430 describes silicone-acrylates obtained by the addition ofhydroxyalkyl acrylate grafts onto silicones comprising chlorosiloxanefunctions. These POSs comprising acrylate and/or methacrylate functionstherefore comprise functional grafts attached to the silicone chain viaSi—O bonds.

U.S. Pat. No. 4,908,274 (=EP-A-0,281,681) concerns silicone-acrylates inwhich the functionalized graft is attached to the silicone chain bymeans of nonhydrolyzable SiC bonds. These silicone-acrylates result fromthe hydrosilylation of allyl glycidyl ether (AGE) and of an epoxide ofvinylcyclohexene (VCMX), in the presence of a platinum catalyst.

The grafted POS thus obtained is reacted with (meth)acrylic acid or a(meth)acrylic acid anhydride. The reaction is catalyzed bydiazabicyclo(2,2,2)octane. This grafting of acrylate or methacrylatefunctions by means of a first epoxy functionalization occurs both onSi—H units located in the chain and on Si—H end units.

FR-A-2,611,729 discloses a method for preparing an acrylate-functionalor methacrylate-functional POS. The starting product used is a POScomprising ≡SiH units present in the silicone chain or at the end of thesilicone chain. It may, for example, be a linear α,ω-trimethylsilylpoly(dimethyl)(methylhydrogen)siloxane POS: MD₁₁₀D^(H) ₅M, that isreacted with allyl glycidyl ether (AGE). The epoxy-functionalized POSobtained is placed in the presence of acrylic acid, of n-butanol, ofMIBK, of hydroquinone and of a chromium triacetate monohydrate-basedcatalyst. The attachment of the acrylic acid to the ether-epoxy graft iscarried out by opening of the epoxy ring.

The article “Makromol. Chem., RAPID COMMUN., 7, 703-707 (1986)”discloses the synthesis of α,ω-bisacrylate POSs obtained from POSscomprising ≡SiH end units that are reacted with AGE in the presence ofchloroplatinic acid. The epoxy-ended POS thus obtained is reacted withmethacrylic acid in the presence of chromium diisopropyl salicylate.This article corresponds to the abovementioned Rhone Poulenc Frenchpatent.

U.S. Pat. No. 6,211,322 (=EP-A-0,940,458 and EP-A-0,940,422) describesPOSs comprising (meth)acrylate groups, obtained from POSs comprisingSi—H units, that are reacted with a polyhydroxylated alkenyl ether offormula:H₂C═CH—(CH₂)₀₋₁₀—O—CH₂—R³—(CH₂—OH)₂₋₁₀in the presence of platinum or rhodium catalysts, with R³═C₁-C₁₀ alkylradical.

The silicone bearing a polyhydroxylated ether graft thus obtained isthen subjected to esterification with (meth)acrylic acid and optionallywith a monocarboxylic acid comprising no double bonds. This“acrylization” of polyhydroxyalkylsiloxane is catalyzed by triflic acid.

J. L. Speier et al., 82, 3601 (1980) and U.S. Pat. Nos. 6,211,322,4,503,208 and 3,767,690 disclose acrylate POSs obtained by reacting anallyloxy polyol with a POS comprising an Si—H unit, in the presence of aplatinum catalyst, as proposed in, can engender unwanted side reactions,with in particular the appearance of propene, unless the silicon hydridecontains electron-donating groups such as chlorine atoms or carbonylgroups.

U.S. Pat. No. 5,981,679 describes POSs carrying (meth)acryloyl groups attheir two ends. In order to obtain these α,ω-bisacrylate silicones, thestarting products used are α,ω-dimethylhydrogensiloxy POSs, which arereacted by hydrosilylation on one of the double bonds of (meth)acrylatecompounds each comprising at least two, preferably three, (meth)acryloylgroups. Conventionally, this hydrosilylation is carried out in thepresence of a metal catalyst, preferably a platinum-based catalyst. ThePOS comprising an SiH unit is preferably an α,ω-diethoxyhydrogensiloxypolydimethylsiloxane obtained from a polydimethylsiloxane-α,ω-diol thatis condensed with triethoxysilane.

FR-A-2,634,769 discloses a diorganopolysiloxane comprising a thioalkylacrylate function obtained by reacting a vinyl POS, for example a linearα,ω-vinyl polydimethylsiloxane, with a mercapto alkanol that reacts withthe vinyl functions by means of the thiol groups, so as to produce anα,ω-thiolalkylhydroxylated polydimethylsiloxane. This alcohol is able toreact with acrylic acid by esterification. The reaction of the thiolwith the vinyl functions of the POS takes place in the presence of afree-radical generator of the azobisisobutyronitrile (AIBN) type.

The unpublished French patent application No. 0108896 of Jun. 29, 2001concerns a polyorganosiloxane (POS) carrying at least one unsaturatedcarboxylic acid ester, preferably (meth)acrylate, group (A),characterized in that it is obtained by reacting at least one POS (I) or(II) carrying at least one ≡Si—H unit with at least one unsaturatedepoxide (III), and then with at least one polyhydroxylated nucleophile(IV) capable of opening the epoxy function(s) involved and, finally,with at least one unsaturated carboxylic acid (V), preferably(meth)acrylic acid, which combines with the hydroxyls of the nucleophile(IV) so as to form the ester groups (A).

These acrylate POSs are obtained, for example, as indicated below:

WO 01/77240 discloses a composition based on functionalized acrylatePOSs, comprising dimethylsiloxy units, trimethylsiloxy endgroups andmethyl-acrylate-siloxy units.

Even more specifically, the (poly)(meth)acrylate POSs that can be usedas additive 3. according to the invention may be those sold under thenames BYK Silclean 3700®, Tego RC 902β®, Tego RC 702, PC 900, PC 911,which are acrylic POSs sold by Rhodia Inc and corresponding to thosedescribed in WO-A-01/77240.

As regards the epoxidized POSs, they comprise at least one epoxy groupper molecule, in the chain and/or at the ends of the chain. Theepoxidized group(s) may, for example, be included in the substituents Xof the silicons having the formula below:

with:

E and D, which are identical or different radicals selected from amonglinear or branched C₁-C₄ alkyl radicals,

z, which is equal to 0 or 1,

R⁹, R¹⁰ and R¹¹, which are identical or different radicals representinghydrogen or a C₁-C₄ linear or branched alkyl radical, hydrogen beingmore particularly preferred,

with the proviso that, alternatively, R⁹ and R¹⁰ or R¹¹ may constitute,together with the two carbons carrying the epoxy, an alkyl ring havingfrom 5 to 7 ring members.

According to yet another preferred embodiment of the invention, thesilylated compound 4, is an epoxidized alkoxysilane, preferablycorresponding to the general formula below:

in which:

R⁷ is a C₁-C₄ linear or branched alkyl radical,

R⁸ is a linear or branched alkyl radical,

y is equal to 0, 1, 2 or 3, preferably to 0 or 1, and even morepreferably to 0,

X* corresponds to the same definition as that given above for X orcorresponds to a group comprising at least one (meth)acrylatefunctionality.

The additive 4. is more preferably selected from the group consistingof:

β-(3,4-epoxycyclohexyl)ethyltriethoxysilane;

3-glycidyloxypropyltriethoxysilane;

3-glycidyloxypropyltrimethoxysilane;

3,4-epoxycyclohexylethyltrimethoxysilane;

3-methacryloxypropyltrimethoxysi lane;

and mixtures thereof.

As examples of silylated compounds 4., mention may be made ofβ-(3,4-epoxycyclohexyl)ethyltriethoxysilane such as that sold by OSIunder the silane registered trademark CoatOSil® 1770,

3-glycidyloxypropyltriethoxysilane such as that sold by Degussa underthe silane registered trademark Dynasilan® Glyeo;

3-glycidyloxypropyltrimethoxysilane such as that sold by Degussa underthe silane registered trademark Dynasilan® Glymo; or alternatively

3-methacryloxypropyltrimethoxysilane such as that sold by Degussa underthe registered trademark Dynasilan® Memo.

As regards the alkenylated and epoxidized and/or alkenyl ether and/oroxetane, silylated compound 5., it is preferable, in accordance with theinvention, to use a compound selected from among epoxy-functional andalkenyl-functional polydiorganosiloxanes comprising at least one unit offormula:X′_(p′)G′_(q′)SiO_(4-(p′+q′)/2)  (VII.1)and at least one unit of formula:X″_(p″)G″_(q″)SiO_(4-(p″+q″)/2)  (VII.2)in which:

X′ comprises at least one group corresponding to the same definition asthat given above for the epoxidized radical X of formula (V) or for theradical Z (E₁, E₂) in formula 1.2,

X″ comprises at least one group corresponding to the same definition asthat given above for the alkenylated radical of formula (IV) as definedabove,

G′ and G″ independently represent a monovalent hydrocarbon-based groupthat has no unfavorable action on the activity of the catalyst and ispreferably selected from among alkyl radicals having from 1 to 8 carbonatoms inclusive, optionally substituted with at least one halogen atom,and advantageously from methyl, ethyl, propyl and 3,3,3-trifluoropropylgroups and also from aryl groups and advantageously from xylyl, tolyland phenyl radicals,

p′=1 or 2,

p″=1 or 2,

q′=0, 1 or 2,

q″=0, 1 or 2,

p′+q′=1, 2 or 3,

p″+q″=1, 2 or 3;

optionally, at least some of the other units of thesepolydiorganosiloxanes are units of mean formula:G_(r)SiO_(4-r/2)  (VIII)in which G has the same meaning as G′ and G″ above, and r has a valuebetween 0 and 3, for example from 1 to 3.

As examples of silylated compounds 5., mention may be made ofpolydimethylsiloxanes functionalized with epoxy and (poly)(meth)acrylateor (poly)(meth)acrylic groups. They may, for example, be an epoxyacrylate silicone resin such as that described in U.S. Pat. No.4,663,185.

The ultrafine filler additive 6. is preferably selected from mineralfillers having a mean particle diameter Φme of close to or less than 0.5μm, advantageously close to or less than 0.1 μm; preferably from:

siliceous fillers belonging to the group of silica powders (colloidalsilicas, pyrogenic and precipitated silicas, or mixtures thereof),

the other mineral fillers selected from the group comprising: TiO₂ andAl₂O₃,

and mixtures thereof.

It may be advantageous, in accordance with the invention, to include atleast one thickener 7. selected from waxes, preferably based onmicronized polyamide.

The varnishes according to the invention can comprise other functionaladditives 8. They may be covering products such as, for example,pigments, dyes (8.1), stabilizers (8.2), in particular UV stabilizers,diluents (solvents) (8.3) or acid rain-resistant agents.

The preferred varnish composition is of the type of those that arecrosslinkable via the cationic route with activation, in particular UVactivation, and comprising, on a dry basis:

1. 99 parts by weight of basic monomer compound 1.1;

2. 0.1 to 1 part by weight of at least one initiator 2. as definedabove;

3. 0 to 2 parts by weight of (meth)acrylic or (meth)acrylate POSs asdefined above;

4. 0 to 2 parts by weight of epoxidized alkoxysilane 4 as defined above;

5. 0 to 2 parts by weight of at least one alkenylated and epoxidizedand/or alkenyl ether and/or oxetane POS as defined above;

6. 0 to 2 parts by weight of at least one ultrafine filler as definedabove;

7. 0 to 2 parts by weight of at least one thickener as defined above;

8. 0 to 1 part by weight of at least one functional additive as definedabove.

The viscosity of the noncrosslinked liquid varnish as it is applied tothe support is an important parameter of the invention. Thus, thisdynamic viscosity η (mPa·s at 25° C.) is such that:

-   -   5≦η≦500,    -   preferably 10≦η≦200,    -   and even more preferably 15≦η≦150.

This dynamic viscosity η at 25° C., known as the “Newtonian” viscosity,is measured, in a manner known per se, at a shear rate gradient of 100s⁻¹ that is sufficiently low for the viscosity measured to beindependent of the rate gradient.

As regards the nature of the various constituents of the siliconevarnish compositions according to the invention, it will be specifiedthat:

1.

or

2.

3. =(poly)acrylate POSs;

4. =β-(3,4-epoxycyclohexyl)ethyltriethoxysilane,3-glycidyloxypropyltriethoxysilane, or epoxidized POS;

5. =epoxy acrylate POS.

According to an advantageous embodiment of the invention, the varnish isin the form of a single-component system capable of rapidly crosslinkingunder UV radiation via the cationic route.

Given the ease with which it is obtained, its low cost and itsanti-fouling properties, the silicone varnishes according to theinvention may have applications in many fields, and in particular in thefield of the coating:

of supports with a woven or nonwoven fibrous core, that may or may notcomprise silicone (i.e., coated on at least one of its faces with atleast one layer of elastomer),

or else of supports of bulk parts made of silicone and/or parts whichmay or may not comprise silicone.

According to another of its aspects, the invention features a varnishingmethod, characterized in that the composition as defined above isapplied, as an anti-fouling varnish, to a support optionally being madeat least in part of silicone, preferably elastomeric silicone.

Preferably, this method consists essentially:

in coating the support using the varnish as defined above,

and in crosslinking the layer of varnish, optionally by thermallyactivating the crosslinking.

According to an advantageous embodiment of the invention, the varnish isapplied to the support according to a coating rate of less than or equalto 35 g/m², preferably between 2 and 25 g/m².

As regards the aspect of use of the varnish according to the invention,it may for example be applied to a support by any appropriate coating ortransfer means (for example, doctor blade, coating cylinder,photogravure, dynamic screen printing, brush, spraying: pistol, etc.).

Crosslinking of the varnish applied to the support to be coated can beactivated, for example, by heating the impregnated, or even coated,support at a temperature of between 50 and 200° C., taking into accountof course the maximum heat resistance of the support.

The thermal activation means are of the type of those that are known andare suitable for this purpose, for example oven or IR radiation.

Other details will be given in this regard in the examples that follow.

The varnishing method defined above can relate either to architecturaltextiles or to supports other than architectural textiles.

The present invention also features the varnish supports (orcomposites), with the possible exclusion of any architectural textile asdefined below, having anti-fouling properties and a low slipcoefficient, that can be obtained via the method as indicated above.This composite is characterized in that it comprises:

a support, preferably a flexible support, and even more preferably asupport selected from the group comprising:

-   -   textiles,    -   nonwoven fibrous supports,    -   polymer films, in particular polyester, polyamide, polyolefin,        polyurethane, polyvinyl chloride or silicone,

optionally, a coating attached to at least one of the faces of thesupport and consisting of at least one layer of silicone elastomer,

at least one layer of varnish based on the compositions as definedabove.

According to a variant, the composition that can be obtained by means ofthe abovementioned method can comprise:

a bulk support optionally made of silicone and/or optionally at leastpartially coated with silicone, the silicone preferably being a siliconeelastomer,

and at least one layer of varnish based on the composition as definedabove.

The silicone coating is optional, for example provided that the supportis itself silicone.

Advantageously, the support of the composite according to the inventioncomprises at least one material selected from the group comprising:

glass in bulk form or in the form of fibers,

ceramics in bulk form or in the form of fibers,

natural or synthetic polymers in bulk form, in the form of fibers, or inthe form of films, in particular polyester, polyamide, polyolefin,polyurethane, polyvinyl chloride or silicone,

cellulosic or lignocellulosic materials in bulk or fibrous form, inparticular papers, cardboards, or the like,

and combinations thereof.

The flexible supports to which the invention relates may be, inter alia,architectural textiles.

Thus, the present invention also features an architectural textile,characterized in that it comprises a composite that can be obtained bymeans of the varnishing method defined above and applied to anarchitectural textile, said composite comprising:

a support, preferably a flexible support, and even more preferably asupport selected from the group comprising:

-   -   textiles,    -   nonwoven fibrous supports,    -   polymer films,

optionally, a coating attached to at least one of the faces of thesupport and consisting of at least one layer of silicone elastomer andat least one other (co)polymer,

at least one layer of varnish as defined above.

Advantageously, the support included in this architectural textilecomprises at least one material selected from the group comprising:

glass in the form of fibers,

ceramics in the form of fibers,

natural or synthetic polymers in the form of fibers or in the form offilms, in particular polyester, polyamide, polyurethane, polyvinylchloride or silicone,

cellulosic or lignocellulosic materials in bulk or fibrous form, inparticular papers, cardboards, or the like.

Other flexible supports to which the invention relates and which aredifferent from the “architectural textiles” may be, inter alia, thoseintended for the production of:

airbags used for protecting the occupants of a vehicle,

glass braids (woven glass sheets for thermal and dielectric protectionfor electrical wires),

conveyor belts, fire-barrier or thermal insulation fabrics,

clothing,

compensators (flexible sealing sleeves for pipe work), etc.

According to another of its aspects, the present invention features:

these manufactured articles that comprise composite as defined above andare different from those that go to make up architectural textiles,

and also the manufactured articles comprising architectural textilesbased on the composite also defined above.

Other flexible supports to which the invention relates and which aredifferent from the “architectural textiles” as defined above may be,inter alia:

airbags used for protecting the occupants of a vehicle,

glass braids (woven glass sheets for thermal and dielectric protectionfor electrical wires),

conveyor belts, fire-barrier or thermal insulation fabrics,

clothing, etc.

The fibrous supports to be coated and then varnished in accordance withthe invention may, for example, be woven fabrics, nonwoven fabrics, orknits, or more generally any fibrous support comprising fibers selectedfrom the group of materials comprising: glass, silica, metals, ceramic,silicon carbide, carbon, boron, natural fibers, such as cotton, wool,hemp or flax, artificial fibers, such as viscose, or cellulose fibers,synthetic fibers, such as polyesters, polyamides, polyacrylics, “chlorofibers”, polyolefins, synthetic rubbers, polyvinyl alcohol, aramides,“fluoro fibers”, phenolics, silicones, etc.

As preferred examples of fibrous supports, mention may be made oftissues made of glass, polyester, polyamide, polyurethane, polyolefin,polyvinyl chloride or silicone.

Besides the silicone-coated flexible textile supports, the anti-foulingvarnish according to the invention can be applied:

to plastic films (e.g., made of polyester), namely thermal transferribbons for printers of the same name,

or to plastic protective packaging films [e.g., made of polyester,polyurethane, polyamide, polyolefin (polyethylene or of polypropylene),polyvinyl chloride or silicone].

The present invention, moreover, also features the use of thecompositions as defined above, as anti-fouling varnishes, for examplefor coating a fibrous support, with the possible exception of anyarchitectural textile.

The present invention also features the use, as an anti-fouling varnish,of a composition that is polymerizable/crosslinkable via the cationicroute and that comprises, per 100 parts by weight:

1. at least 80 parts by weight of at least one basic compound 1. asdefined above;

2. from 0.1 to 10 parts by weight of at least one cationic initiator 2.as defined above;

3. from 0 to 10 parts by weight of at least one silylated compound asdefined above and bearing, per molecule, at least one alkenylatedsubstituent, preferably (meth)acrylic or a salt thereof;

4. from 0 to 10 parts by weight of at least one silylated compound asdefined above and carrying, per molecule, at least one epoxy group;

5. from 0 to 10 parts by weight of at least one silylated compound asdefined above and bearing, per molecule, at least one alkenylatedsubstitutent, preferably (meth)acrylic or a salt thereof, and at leastone epoxy, alkenyl ether or oxetane group;

6. from 0 to 10 parts by weight of at least one ultrafine filler asdefined above;

7. from 0 to 10 parts by weight of at least one thickener as definedabove;

8. from 0 to 10 parts by weight of at least one other functionaladditive as defined above; for forming an architectural textile.

The bulk supports to which the invention relates may be, inter alia,parts selected from the group comprising:

furniture,

claddings,

billboards,

windshields,

compensators (flexible sealing sleeves for pipe work),

or filter panels.

Finally, the present invention features any manufactured articlecomprising composite as defined above.

The silicone capable of forming the coating or the bulk part to whichthe varnish composition according to the invention can be applied may bean elastomer based on polyorganosiloxane(s), which is crosslinkable orat least partially crosslinked, and preferably selected from:

polyaddition or polycondensation RTV silicones,

and/or peroxide EVC silicones,

and/or polyaddition LSR silicones.

The anti-fouling varnish obtained from the composition as defined aboveis applied to the (upper) layer(s) of silicone elastomer.

The expressions “RTV”, “LSR” and “EVC” are well known to those skilledin the art; RTV is the abbreviation for “Room Temperature Vulcanizing”,LSR is the abbreviation for “Liquid Silicone Rubber” and EVC is theabbreviation for “Elastomère Vulcanisable à Chaud [Hot VulcanizingElastomer]”.

In practice, the invention is directed more precisely to the supports(for example, textiles such as those used for the production of airbags)coated on one and/or the other of their faces with a layer of RTV, EVCor LSR crosslinked silicone elastomer, itself coated with a coating ofanti-fouling silicone varnish as defined above.

The problem of introducing anti-fouling properties is particularly acuteas regards these crosslinked silicone elastomer coatings since, as hasalready been indicated above, the latter have the characteristic ofhaving a sticky feel.

The polyorganosiloxanes, main constituents of the adhesive layers ofcrosslinked elastomers or of the bulk supports/parts to which thevarnish according to the invention may be applied, can be linear,branched or crosslinked, and can comprise hydrocarbon-based radicalsand/or reactive groups such as, for example, hydroxyl groups,hydrolyzable groups, alkenylated groups and hydrogen atoms. It should benoted that polyorganosiloxane compositions are thoroughly described inthe literature, and in particular in the text by Walter Noll: “Chemistryand Technology of Silicones”, Academic Press, 1968, 2nd edition, pages386 to 409.

More precisely, these varnishable polyorganosiloxanes comprise siloxylunits of general formula:

$\begin{matrix}{{R{^\circ}}_{n\; 1}{SiO}_{\frac{4 - n_{1}}{2}}} & \left( I^{\prime} \right)\end{matrix}$and/or of siloxyl units of formula:

$\begin{matrix}{{Z{^\circ}}_{x_{1}}{R{^\circ}}_{y_{1}}{SiO}_{\frac{4 - x_{1} - y_{1}}{2}}} & \left( {II}^{\prime} \right)\end{matrix}$in which formulae, the various symbols have the following meanings:

the symbols R^(o), which may be identical or different, are each a groupthat is hydrocarbon-based and nonhydrolyzable in nature, it beingpossible for this radical to be:

-   -   an alkyl or haloalkyl radical having from 1 to 5 carbon atoms        and containing from 1 to 6 chlorine and/or fluorine atoms,    -   cycloalkyl and halocycloalkyl radicals having from 3 to 8 carbon        atoms and containing from 1 to 4 chlorine and/or fluorine atoms,    -   aryl, alkylaryl and haloaryl radicals having from 6 to 8 carbon        atoms and containing from 1 to 4 chlorine and/or fluorine atoms,    -   cyanoalkyl radicals having from 3 to 4 carbon atoms;

the symbols Z^(o), which may be identical or different, are each ahydrogen atom, a C₂-C₆ alkenyl radical, a hydroxyl group, a hydrolyzableatom or a hydrolyzable group;

n₁=an integer equal to 0, 1, 2 or 3;

x₁=an integer equal to 0, 1, 2 or 3;

y₁=an integer equal to 0, 1 or 2;

the sum x+y ranges from 1 to 3.

By way of illustration, mention may be made, among the organic radicalsR^(o) directly attached to the silicon atoms, of: methyl; ethyl; propyl;isopropyl; butyl; isobutyl; n-pentyl; t-butyl; chloromethyl;dichloromethyl; α-chloroethyl; α,β-dichloroethyl; fluoromethyl;difluoromethyl; α,β-difluoroethyl; 3,3,3-trifluoropropyl;trifluorocyclopropyl; 4,4,4-trifluorobutyl;3,3,4,4,5,5-hexafluoropentyl; β-cyanoethyl; γ-cyanopropyl; phenyl;p-chlorophenyl; m-chlorophenyl; 3,5-dichlorophenyl; trichlorophenyl;tetrachlorophenyl; o-, p- or m-tolyl or α,α,α-trifluorotolyl groups; andxylyl groups such as 2,3-dimethylphenyl or 3,4-dimethylphenyl.

Preferably, the organic radicals R^(o) attached to the silicon atoms aremethyl or phenyl radicals, it being possible for these radicals to beoptionally halogenated, or else cyanoalkyl radicals.

The symbols Z^(o) may be hydrogen atoms, hydrolyzable atoms such ashalogen atoms, in particular chlorine atoms, vinyl groups, hydroxylgroups or hydrolyzable groups such as, for example: amino, amido,aminoxy, oxime, alkoxy, alkenyloxy or acyloxy.

The nature of the polyorganosiloxane and therefore the ratios of thesiloxyl units (I′) to the siloxyl units (II″), and the distribution ofthe latter, are, as is known, selected according to the crosslinkingtreatment that will be carried out on the curable (or vulcanisable)composition for the purpose of converting it to an elastomer.

It is possible to use a great variety of one-component or two-componentcompositions that crosslink by means of polyaddition or polycondensationreactions, in the presence of a metal catalyst and, optionally, of anamine and a crosslinking agent.

Two-component or one-component polyorganosiloxane compositions thatcrosslink at ambient temperature (RTV) or under heat (EVC) by means ofpolyaddition reactions, essentially by reaction of hydrosilyl groupswith alkenylsilyl groups, generally in the presence of a metal catalyst,preferably a platinum catalyst, are described, for example, in U.S. Pat.Nos. 3,220,972, 3,284,406, 3,436,366, 3,697,473 and 4,340,709. Thepolyorganosiloxanes that go to make up these compositions generally arepairs based, firstly, on a linear, branched or crosslinked polysiloxaneof units (II) in which the residue Z^(o) represents a C₂-C₆ alkenylgroup and where x₁ is at least equal to 1, optionally in combinationwith units (I′), and, secondly, on a linear, branched or crosslinkedhydropolysiloxane comprising units (II′) in which the residue Z^(o) thenrepresents a hydrogen atom and where x₁ is at least equal to 1,optionally in combination with units (I′).

Two-component or one-component polyorganosiloxane compositions thatcrosslink at ambient temperature (RTV) by means of polycondensationreactions under the action of moisture, generally in the presence of ametal catalyst, for example a tin compound, are described for example,for the one-component compositions, in U.S. Pat. Nos. 3,065,194,3,542,901, 3,779,986 and 4,417,042, and in FR-A-2,638,752, and, for thetwo-component compositions, in U.S. Pat. Nos. 3,678,002, 3,888,815,3,933,729 and 4,064,096. The polyorganosiloxanes that go into making upthese compositions are generally linear, branched or crosslinkedpolysiloxanes comprising units (II′) in which the residue Z^(o) is ahydroxyl group or an atom or a hydrolyzable group and where x₁ is atleast equal to 1, with the possibility of having at least one residueZ^(o) which is equal to a hydroxyl group or to an atom or to ahydrolyzable group and at least one residue Z^(o) which is equal to analkenyl group when x₁ is equal to 2 or 3, said units (II′) beingoptionally in combination with units (I′). Similar compositions may alsocontain a crosslinking agent which is in particular a silane bearing atleast three hydrolyzable groups, for instance a silicate, analkyltrialkoxysilane or an aminoalkyltrialkoxysilane.

These RTV polyorganosiloxane compositions that crosslink by means ofpolyaddition or polycondensation reactions advantageously have aviscosity at 25° C. that is at most equal to 100,000 mPa·s, andpreferably between 10 and 50,000 mPa·s.

It is possible to use RTV compositions that crosslink at ambienttemperature by means of polyaddition or polycondensation reactions, thathave a viscosity at 25° C. of greater than 100,000 mPa·s, such as thatwhich is in the range that goes from a value greater than 100,000 mPa·sto 300,000 mPa·s; this method is recommended when it is desired toprepare curable compositions charged with fillers in which the filler(s)used has(have) a tendency to separate by sedimentation.

It is also possible to use compositions that crosslink under heat bymeans of polyaddition reactions, and more precisely “polyadditionEVC-type” compositions, having a viscosity at 25° C. that is at leastequal to 500,000 mPa·s, and preferably between 1 million mPa·s and 10million mPa·s, and even more.

The compositions may also be compositions that are curable at hightemperature under the action of organic peroxides such as2,4-dichlorobenzoyl peroxide, benzoyl peroxide, t-butyl perbenzoate,cumyl peroxide or di-t-butyl peroxide. The polyorganosiloxane or gumthat goes into making up such compositions (simply referred to as EVCtype) then consists essentially of siloxyl units (I′), optionally incombination with units (II′) in which the residue Z^(o) represents aC₂-C₆ alkenyl group and where x is equal to 1. Such EVCs are, forexample, described in U.S. Pat. Nos. 3,142,655, 3,821,140, 3,836,489 and3,839,266. These compositions advantageously have a viscosity at 25° C.that is at least equal to 1 million mPa·s, and preferably between 2million and 10 million mPa·s, and even more.

Other polyorganosiloxane compositions that can be varnished with thesilicone varnish composition according to the invention are those,one-component or two-component, that crosslink under heat by means ofpolyaddition reactions, called LSR compositions. These compositionscorrespond to the definitions given above with respect to the preferredcompositions called RTVs, except with regard to their viscosity, whichthis time is in the range that goes from a value greater than 100,000mPa·s to 500,000 mPa·s.

Without this being limiting, the elastomer silicone coatings to whichthe anti-fouling varnish according to the invention can be applied aremore especially coatings obtained using room temperature vulcanizing,RTV, silicone elastomer compositions, in particular of two-componenttype (RTV 2), by polyaddition.

In order to further illustrate the present invention and the advantagesthereof, the following specific examples are given, it being understoodthat same are intended only as illustrative and in nowise limitative. Insaid examples to follow, all parts and percentages are given by weight,unless otherwise indicated.

EXAMPLES Tests

Good wetting is the condition necessary for even coating with thevarnish; the assessment of this covering is completed by means of anevaluation of the resistance to fouling that it provides.

Resistance to Fouling:

Fouling Test:

The anti-fouling is measured by applying flame black to the varnishcoating and wiping the dirt using absorbent paper of the wadding type.The ability of this support to be more or less readily cleaned is gradedfrom 0 to 5 on a fouling scale (see FIG. 1) according to a comparisonwith infra-type micrographs:

-   -   0=remains black; 5=few black traces remain.

Bonding Ability: Adhesive Strength:

The assembly properties are determined by measuring the adhesivestrength of an EVC. The assembly principle is given below.

Principle of the adhesion test: A sheet of EVC 1 mm thick (generally ofRT21 type) reinforced with a textile cloth is deposited at the surfaceof the fabric coated with RTV and with the varnish. This complex is thenpressed for 3 minutes at 180° C. in order to ensure crosslinking of theEVC, and then the adhesion between the varnish and the EVC is tested bymeans of a peeling test. A force is measured and the location of thebreaking is determined.

Slipping:

The slip coefficients Ks and Kd are determined according to theAPL/END/ET/T219 procedure on coated tissue.

Visual Appearance:

It is noted whether the varnish confers a glossy or matt appearance.

Support:

1. The support sample is an RTV II coating applied to a polyamide 700dctex fabric impregnated with RTV 1530 (grammage 45 g/m²) corona treatedbeforehand.

This RTV II coating is prepared as follows:

40 kg of an α,ω-divinyl silicone oil having a viscosity of 1.5 Pa·s,that gives a titer of 0.1 meq of vinyl (Vi) per gram of oil, 0.24 kg ofdrinking water and 0.24 kg of hexamethyldisilazane are introduced into a100 l arm mixer. After homogenization, 13.9 kg of a pyrogenic silica,characterized by its specific surface area of 200 m²/g, are addedportionwise in about 2 hours. After mixing for approximately 1 hour,2.27 kg of hexamethyldisilazane are again added, in about 1 hour. Twohours later, a heating phase is commenced, in the course of which themixture is placed under a stream of nitrogen (30 m³/h); the heatingcontinues until approximately 140° C. is reached, which plateautemperature is maintained for 2 hours in order to evacuate the volatilesubstances from the composition. The suspension is then allowed to cool.

Starting from this suspension, a part A and a part B are formulated inappropriate reactors.

Part A Contains:

320 g of the suspension,

111 g of an α,ω-divinyl oil with a viscosity of 100 Pa·s, which gives atiter of 0.03 meq Vi per gram of oil,

35 g of ground quartz with a mean particle size (d50) close to 2.5 μm,

12 g of a polyhydro oil with a viscosity of 0.3 Pa·s, which gives atiter of 1.6 meq SiH per gram of oil,

12 g of an α,ω-dihydro oil, which gives a titer of 1.9 meq SiH per gramof oil,

5 g of γ-methacryloxypropyl trimethoxysilane,

5 g of γ-glycidoxypropyl trimethoxysilane,

0.7 g of ethynylcyclohexanol.

Part B Contains:

480 g of the suspension,

20 g of butyl orthotitanate,

1.1 g of a Karstedt catalyst containing 10% of platinum.

Parts A and B are mixed in a ratio of 100 to 10 and, after removal ofbubbles, the test samples required for measuring the mechanicalproperties and the adhesive properties are prepared.

The crosslinking on the support under consideration is carried out bymeans of a 10 minute period in a ventilated oven maintained at 150° C.

The thickness of the coating is sufficient (approximately 300 μm) forthe coated surface to be smooth and for the nature of the fabric used tobecome completely screened.

2. The varnish formulations are coated with a Meyer bar. The layer ofvarnish has a grammage on the order of 15 g/m².

The polymerization is carried out on an IST UV bench (2H-type lamps of160 W power), with a 20 m/min speed of travel.

EXAMPLES

The basic formulation of the varnish includes:

1. of the basic monomer compound Cyracure® 6105 from the company DowChemical:

1. or of the compound S200 sold by Rhodia:

2. of the initiator=cata 211

3. and/or 4. and/or 5. and/or 6. and/or 7. and/or 8.

3. polydimethylsiloxane (PDMS) Byk 3700® sold by Tego Goldschmidt,

3. PDMS acrylate Tego RC 902 sold by Tego Goldschmidt,

3. PDMS acrylate Tego RC 726 sold by Tego Goldschmidt,

3. PDMS acrylate PC 911,

4. Coatosil 1770® sold by Crompton:β-(3,4-epoxycyclohexyl)ethyltriethoxysilane,

4. glycidyloxypropyltrimethoxysilane,

4. RCA 200 sold by Rhodia:

with n=100

4. poly 200 sold by Rhodia: mixture of siloxanes, the viscosity of whichis 23.5 mPa·s and for which the proportions by weight and formulae B₁,B₂ and B₃ are given below:

with 89% of B₁ where a=0; 9% of B₁ where a=1; 0.2% of B₁ where a=2;

with 0.3% of B₂ where a=0;

and with 1.5% of B₃ where a=O and b=1.

5. PDMS epoxy acrylate as described by or as obtained by means of U.S.Pat. No. 4,663,185.

All the results obtained are reported in the following Tables 1, 2 and3.

TABLE 1 Type of constit- TRIAL uent A B C D Cyracure ® 1 9.9 9.9 9.9 9.96105 Byk 3700 3 0.07 0.05 PC911 3 0.08 Coatosil ® 4 0.04 0.03 1770 RCA ®200 4 Cata 211 2 0.3 0.3 0.3 0.3 % additive 0.4% 0.0% 1.0% 0.3%Miscibility OK borderline OK OK Bar 2 2 2 2 Number 1/2* 20 m/minirradiation/ 160 W/ power/speed Appearance borderline OK borderlineborderline Thickness 13-18 11-18 12-18 13-19 (micron) Kd 0.17 0.15 0.150.11 Test 3.5 5 4 3 consisting of flame black before bonding EVC*bonding Mean 65 27 70 45 adhesive strength (N/5 cm) Breaking fabric/fabric/ fabric/ fabric/ varnish EVC varnish varnish

TABLE 2 Type of constit- TRIAL uent E F G H Cyracure ® 1 9.9 9.9 9.9 9.96105 Byk 3700 3 0.07 PC911 3 0.06 0.06 0.06 Coatosil ® 4 0.1 0.2 0.11770 PDMS 5 0.1 epoxyacrylate Cata 211 2 0.3 0.3 0.3 % additive 1.6%2.5% 2.2% 1.0% Miscibility Borderline borderline Borderline BorderlineBar 2 2 2 2 Number irradiation/ power/speed Appearance OK Borderline OKOK Thickness (micron) Kd 0.80 0.80 0.59 0.77 Test 4 4 4 5 consisting offlame black before bonding EVC* bonding Mean 70 122 70 >=71 adhesivestrength (N/5 cm) Breaking EVC/ varnish/ EVC/ EVC/ varnish fabricvarnish varnish

The varnish formulations that make it possible to obtain the desiredperformance levels score at least 4 in the fouling test, have a Kd<0.8and allow an adhesion level>70 N.

They comprise: cyracure 1./cata211 2./an acrylate PDMS 3. and anepoxidized alkoxysilane 4.

A positive trial h was realized using a PDMS having a double acrylateand epoxide functionality as additive 5.

An additional trial i was realized by replacing the Cyracure®1. with thepolymer S200 1.; this trial is conclusive.

TABLE 3 Type of TRIAL constituent I S200 1 9.9 PC911 3 0.06 Coatosil ®1770 4 0.1 Cata 211 2 0.3 % additive 1.6% Miscibility borderline Bar 2Appearance OK Kd 0.80 Test consisting of 4 flame black before bondingMean adhesive strength 70 (N/5 cm) Breaking EVC/varnish

Each patent, patent application, publication and literaturearticle/report cited or indicated herein is hereby expresslyincorporated by reference.

While the invention has been described in terms of various specific andpreferred embodiments, the skilled artisan will appreciate that variousmodifications, substitutions, omissions, and changes may be made withoutdeparting from the spirit thereof. Accordingly, it is intended that thescope of the present invention be limited solely by the scope of thefollowing claims, including equivalents thereof.

1. A process for varnishing a support substrate other than anarchitectural textile, comprising: coating an anti-fouling varnishcomposition onto a silicone face surface of a support substrate composedat least in part of a silicone, wherein the anti-fouling varnishcomposition comprises: A. at least one alkenylsilane; B. at least onecatalytic system comprising: B/1 at least one organometalliccondensation catalyst; B/2 at least one metal M chelate and/or at leastone metal alkoxide of general formula M(OJ)_(n), wherein n=valence of Mand J=linear or branched C₁-C₈ alkyl radical, M being selected from thegroup consisting of Ti, Zr, Ge and Al; C. at least one ultrafine filler;D. at least one arylsilane other than A; E. at least one other silaneother than A and other than D; F. optionally, at least one thickeningagent; and G. optionally, at least one functional additive, onto asilicone face surface of a support substrate composed at least in partof a silicone.
 2. The process for varnishing as defined by claim 1,wherein the face surface of the support substrate comprises at least onenonsilicone (co)polymer.
 3. The process as defined by claim 1, furthercomprising; crosslinking the layer of varnish composition.
 4. Theprocess as defined by claim 1, wherein the coating is in an amount ofless than or equal to 35 g/m².
 5. A process for varnishing anarchitectural textile, comprising: coating an anti-fouling varnishcomposition onto a silicone face surface of a support substrate composedat least in part of a silicone, wherein the anti-fouling varnishcomposition comprises: A. at least one alkenylsilane; B. at least onecatalytic system comprising: B/1 at least one organometalliccondensation catalyst; B/2 at least one metal M chelate and/or at leastone metal alkoxide of general formula M(OJ)_(n), wherein n=valence of Mand J=linear or branched C₁-C₈ alkyl radical, M being selected from thegroup consisting of Ti, Zr, Ge and Al; C. at least one ultrafine filler;D. at least one arylsilane other than A; E. at least one other silaneother than A and other than D; F. optionally, at least one thickeningagent; and G. optionally, at least one functional additive, onto asilicone face surface of a support substrate composed at least in partof a silicone.
 6. The process for varnishing as defined by claim 5,wherein the face surface of the support substrate comprises at least onenonsilicone (co)polymer.
 7. The process as defined by claim 5, furthercomprising; crosslinking the layer of varnish composition.
 8. Theprocess as defined by claim 5, wherein the coating is in an amount ofless than or equal to 35 g/m².